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    1. Swirsky, DM; Richards, SJ
      Laboratory diagnosis of acute myeloid leukaemia

      BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
    2. Biagini, P; Gallian, P; Attoui, H; Cantaloube, JF; Touinssi, M; de Micco, P; de Lamballerie, X
      Comparison of systems performance for TT virus detection using PCR primer sets located in non-coding and coding regions of the viral genome

      JOURNAL OF CLINICAL VIROLOGY
    3. Siles-Lucas, M; Gottstein, B
      Review: Molecular tools for the diagnosis of cystic and alveolar echinococcosis

      TROPICAL MEDICINE & INTERNATIONAL HEALTH
    4. Gasser, T; Dichgans, M; Finsterer, J; Hausmanowa-Petrusewicz, I; Jurkat-Rott, K; Klopstock, T; Leguern, E; Lehesjoki, AE; Lehmann-Horn, F; Lynch, T; Morris, H; Rossor, M; Steinlein, OK; Wood, N; Zaremba, J; Zeviani, M; Zoharn, A
      EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - Second of two parts

      EUROPEAN JOURNAL OF NEUROLOGY
    5. Gasser, T; Dichgans, M; Finsterer, J; Hausmanowa-Petrusewicz, I; Jurkat-Rott, K; Klopstock, T; LeGuern, E; Lehesjoki, AE; Lehmann-Horn, F; Lynch, T; Morris, H; Rossor, M; Steinlein, OK; Wood, N; Zaremba, J; Zeviani, M; Zoharn, A
      EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - First of two parts

      EUROPEAN JOURNAL OF NEUROLOGY
    6. Strippoli, P; Sarchielli, S; Santucci, R; Bagnara, GP; Brandi, G; Biasco, G
      Cold single-strand conformation polymorphism analysis: Optimization for detection of APC gene mutations in patients with familial adenomatous polyposis

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    7. Heim, RA; Sugarman, EA; Allitto, BA
      Improved detection of cystic fibrosis mutations in the heterogeneous US population using an expanded, pan-ethnic mutation panel

      GENETICS IN MEDICINE
    8. Shahidi-Asl, M; Krause, JR
      Molecular pathology of non-Hodgkin lymphomas

      JOURNAL OF CLINICAL LIGAND ASSAY
    9. Feriotto, G; Ferlini, A; Ravani, A; Calzolari, E; Mischiati, C; Bianchi, N; Gambari, R
      Biosensor technology for real-time detection of the cystic fibrosis W1282Xmutation in CFTR

      HUMAN MUTATION
    10. Kubota, T; Horie, M; Takano, M; Yoshida, H; Takenaka, K; Watanabe, E; Tsuchiya, T; Otani, H; Sasayama, S
      Evidence for a single nucleotide polymorphism in the KCNQ1 potassium channel that underlies susceptibility to life-threatening arrhythmias

      JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY
    11. Surin, VL; Luk'yanenko, AV; Karpova, IV; Misyurin, AV; Pustovoit, YS; Pivnik, AV
      Three novel mutations in porphobilinogen deaminase gene identified in Russian patients with acute intermittent porphyria

      RUSSIAN JOURNAL OF GENETICS
    12. Beardall, J; Young, E; Roberts, S
      Approaches for determining phytoplankton nutrient limitation

      AQUATIC SCIENCES
    13. Datar, RH
      Nucleic acids in diagnosis (Part II): Genetic testing and screening

      NATIONAL MEDICAL JOURNAL OF INDIA
    14. Hassmann, J; Misch, A; Schulein, J; Krause, J; Grassl, B; Muller, P; Bertling, WM
      Development of a molecular diagnosis assay based on electrohybridization at plastic electrodes and subsequent PCR

      BIOSENSORS & BIOELECTRONICS
    15. Ladanyi, M; Lui, MY; Antonescu, CR; Krause-Boehm, A; Meindl, A; Argani, P; Healey, JH; Ueda, T; Yoshikawa, H; Meloni-Ehrig, A; Sorensen, PHB; Mertens, F; Mandahl, N; van den Berghe, H; Sciot, R; Dal Cin, P; Bridge, J
      The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25

      ONCOGENE
    16. Qin, XA; Urdahl, KB
      PCR and sequencing of independent genetic targets for the diagnosis of culture negative bacterial endocarditis

      DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE
    17. Kuwahara, T; Norimatsu, I; Nakayama, H; Akimoto, S; Kataoka, K; Arimochi, H; Ohnishi, Y
      Genetic variation in 16S-23S rDNA internal transcribed spacer regions and the possible use of this genetic variation for molecular diagnosis of Bacteroides species

      MICROBIOLOGY AND IMMUNOLOGY
    18. Pistorius, S; Schackert, HK; Saeger, HD
      Hereditary colorectal carcinomas - Reflection on preventive surgery

      ONKOLOGIE
    19. Maurer, B; Gromoll, J; Simoni, M; Nieschlag, E
      Prevalence of Y chromosome microdeletions in infertile men who consulted atertiary care medical centre: the Munster experience

      ANDROLOGIA
    20. Heninger, E; Otto, E; Imm, A; Caridi, G; Hildebrandt, F
      Improved strategy for molecular genetic diagnostics in juvenile nephronophthisis

      AMERICAN JOURNAL OF KIDNEY DISEASES
    21. van Golde, RJT; Wetzels, AMM; de Graaf, R; Tuerlings, JHAM; Braat, DDM; Kremer, JAM
      Decreased fertilization rate and embryo quality after ICSI in oligozoospermic men with microdeletions in the azoospermia factor c region of the Y chromosome

      HUMAN REPRODUCTION
    22. Liow, SL; Yong, EL; Ng, SC
      Prognostic value of Y deletion analysis - How reliable is the outcome of Ydeletion analysis in providing a sound prognosis?

      HUMAN REPRODUCTION
    23. Curigliano, G; Ferretti, G; Flamini, G; Goldhirsch, A; de Braud, F; Calabro, MG; Mandaly, M; Nole, F; De Pas, T; D'Addessi, A; Cittadini, A
      Diagnosis of T1 bladder transitional cell carcinoma by denaturing gradientgel electrophoresis urinalysis

      ANTICANCER RESEARCH
    24. Nikitin, EA; Leniva, EA; Sudarikov, AB
      Role of molecular methods in the diagnosis and monitoring of lympho proliferative diseases

      GEMATOLOGIYA I TRANSFUZIOLOGIYA
    25. Dries, V; Odenthal, M; Schirmacher, P; Dienes, HP
      Liver biopsy in chronic hepatitis C Histopathology, molecular diagnostic analysis, and implications for therapeutic management

      PATHOLOGE
    26. Bosserhoff, AK; Hellerbrand, C; Buettner, R
      Clinical and genetic aspects of hereditary hemochromatosis

      PATHOLOGE
    27. Tannapfel, A
      Molecular pathology of gastric carcinoma: current state of research

      PATHOLOGE
    28. Barlic-Maganja, D; Grom, J
      Highly sensitive one-tube RT-PCR and microplate hybridisation assay for the detection and for the discrimination of classical swine fever virus from other pestiviruses

      JOURNAL OF VIROLOGICAL METHODS
    29. Judge, DP; Biery, NJ; Dietz, HC
      Characterization of microsatellite markers flanking FBN1: Utility in the diagnostic evaluation for Marfan syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    30. Felice, KJ; Moore, SA
      Unusual clinical presentations in patients harboring the facioscapulohumeral dystrophy 4q35 deletion

      MUSCLE & NERVE
    31. Tzschach, A; Thamm, B; Imthurn, B; Weber, W; Alexander, H; Glander, HJ; Froster, U
      Absence of Yq microdeletions in infertile men

      ARCHIVES OF ANDROLOGY
    32. Rey, L; Lambert, V; Wattre, P; Andreoletti, L
      Detection of enteroviruses ribonucleic acid sequences in endomyocardial tissue from adult patients with chronic dilated cardiomyopathy by a rapid RT-PCR and hybridization assay

      JOURNAL OF MEDICAL VIROLOGY
    33. Rha, SH; Dong, SM; Jen, J; Nicol, T; Sidransky, D
      Molecular detection of cervical intraepithelial neoplasia and cervical carcinoma by microsatellite analysis of Papanicolaou smears

      INTERNATIONAL JOURNAL OF CANCER
    34. Kubicka, S; Kuhnel, F; Flemming, P; Hain, B; Kezmic, N; Rudolph, KL; Manns, M; Meier, PN
      K-ras mutations in the bile of patients with primary sclerosing cholangitis

      GUT
    35. Boutin, P; Vasseur, F; Samson, C; Wahl, C; Froguel, P
      Routine mutation screening of HNF-1 alpha and GCK genes in MODY diagnosis:How effective are the techniques of DHPLC and direct sequencing used in combination?

      DIABETOLOGIA
    36. Sun, CF; Lee, CH; Cheng, SW; Lin, MH; Wu, TL; Tsao, KC; Chiu, DTY; Liou, JD; Chu, DC
      Real-time quantitative PCR analysis for alpha-thalassemia-1 of Southeast Asian type deletion in Taiwan

      CLINICAL GENETICS
    37. Latour, P; Boutrand, L; Levy, N; Bernard, R; Boyer, A; Claustrat, F; Chazot, G; Boucherat, M; Vandenberghe, A
      Polymorphic short tandem repeats for diagnosis of the Charcot-Marie-Tooth IA duplication

      CLINICAL CHEMISTRY
    38. Burnett, JR; Moses, EA; Coft, KD; Brown, AJ; Grainger, K; Vasikaran, SD; Leitersdorf, E; Watts, GF
      Clinical and biochemical features, molecular diagnosis and long-term management of a case of cerebrotendinous xanthomatosis

      CLINICA CHIMICA ACTA
    39. Lynch, HT
      Family information service and hereditary cancer

      CANCER
    40. Gilmour, J; Skuse, D; Pembrey, M
      Hyperphagic short stature and Prader-Willi syndrome: a comparison of behavioural phenotypes, genotypes and indices of stress

      BRITISH JOURNAL OF PSYCHIATRY
    41. Takano, T; Miyauchi, A; Yoshida, H; Hasegawa, Y; Kuma, K; Amino, N
      Quantitative measurement of thyroglobulin mRNA in peripheral blood of patients after total thyroidectomy

      BRITISH JOURNAL OF CANCER
    42. Alcantara, MA; Garcia-Cavazos, R; Hernandez, E; Gonzales-del Angel, A; Carnevale, A; Orozco, L
      Carrier detection and prenatal molecular diagnosis in a Duchenne muscular dystrophy family without any affected relative available

      ANNALES DE GENETIQUE
    43. Silverstein, S; Lerer, I; Buiting, K; Abeliovich, D
      The 28-kb deletion spanning D15S63 is a polymorphic variant in the Ashkenazi Jewish population

      AMERICAN JOURNAL OF HUMAN GENETICS
    44. Aho, M; Harkonen, K; Suikkari, AM; Juvonen, V; Anttila, L; Lahdetie, J
      Y-chromosomal microdeletions among infertile Finnish men

      ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA
    45. Laleman, W; Vanderschueren, S; Mortelmans, L; Knockaert, DC
      Progressive bouts of acute abdomen: Pet the peritoneum

      ACTA CLINICA BELGICA
    46. Avidor, B; Varon, M; Marmor, S; Lifschitz-Mercer, B; Kletter, Y; Ephros, M; Giladi, M
      DNA amplification for the diagnosis of cat-scratch disease in small-quantity clinical specimens

      AJCP. American journal of clinical pathology
    47. Fridman, C; Koiffmann, CP
      Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes

      GENETICS AND MOLECULAR BIOLOGY
    48. Costa, MRE; Lacaz, CD; Kawasaki, M; De Camargo, ZP
      Conventional versus molecular diagnostic tests

      MEDICAL MYCOLOGY
    49. Carter, JS; Kemp, DJ
      A colorimetric detection system for Calymmatobacterium granulomatis

      SEXUALLY TRANSMITTED INFECTIONS
    50. Ramdall, RB; Cunha, L; Astrin, KH; Katz, DR; Anderson, KE; Glucksman, M; Bottomley, SS; Desnick, RJ
      Acute intermittent porphyria: novel missense mutations in the human hydroxymethylbilane synthase gene

      GENETICS IN MEDICINE
    51. Fridman, C; Varela, MC; Kok, F; Setian, N; Koiffmann, CP
      Prader-Willi syndrome: Genetic tests and clinical findings

      GENETIC TESTING
    52. Brown, SA; Mitchell, M; Cutler, JA; Moore, G; Smith, MP; Savidge, GF
      Rapid genetic diagnosis in neonatal pulmonary artery thrombosis caused by homozygous antithrombin Budapest 3

      CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
    53. Gerald, WL
      A practical approach to the differential diagnosis of small round cell tumors of infancy using recent scientific and technical advances

      INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY
    54. Gastier, JM; Berg, MA; Vesterhus, P; Reiter, EO; Francke, U
      Diverse deletions in the growth hormone receptor gene cause growth hormoneinsensitivity syndrome

      HUMAN MUTATION
    55. Nagasaka, T; Lai, R; Chen, YY; Chen, WG; Arber, DA; Chang, KL; Weiss, LM
      The use of archival bone marrow specimens in detecting B-cell non-Hodgkin's lymphomas using polymerase chain reaction methods

      LEUKEMIA & LYMPHOMA
    56. Cailloux, F; Gauthier-Barichard, F; Mimault, C; Isabelle, V; Courtois, V; Giraud, G; Dastugue, B; Boespflug-Tanguy, O
      Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    57. Bedendo, IP; Davis, RE; Dally, EL
      Detection and identification of the maize bushy stunt phytoplasma in corn plants in Brazil using PCR and RFLP

      INTERNATIONAL JOURNAL OF PEST MANAGEMENT
    58. Brown, RL; Pollock, AN; Couchman, KG; Hodges, M; Hutchinson, DO; Waaka, R; Lynch, P; McCarthy, TV; Stowell, KM
      A novel ryanodine receptor mutation and genotype-phenotype correlation in a large malignant hyperthermia New Zealand Maori pedigree

      HUMAN MOLECULAR GENETICS
    59. Roof, E; Stone, W; MacLean, W; Feurer, ID; Thompson, T; Butler, MG
      Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes

      JOURNAL OF INTELLECTUAL DISABILITY RESEARCH
    60. Darras, BT; Jones, HR
      Diagnosis of pediatric neuromuscular disorders in the era of DNA analysis

      PEDIATRIC NEUROLOGY
    61. Atobe, JH; Hirata, MH; Hoshino-Shimizu, S; Schmal, MR; Mamizuka, EM
      One-step heminested PCR for amplification of Neisseria meningitidis DNA incerebrospinal fluid

      JOURNAL OF CLINICAL LABORATORY ANALYSIS
    62. Maurer, B; Simoni, M
      Y chromosome microdeletion screening in infertile men

      JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    63. Paton, DJ; McGoldrick, A; Bensaude, E; Belak, S; Mittelholzer, C; Koenen, F; Vanderhallen, H; Greiser-Wilke, I; Scheibner, H; Stadejek, T; Hofmann, M; Thuer, B
      Classical swine fever virus: a second ring test to evaluate RT-PCR detection methods

      VETERINARY MICROBIOLOGY
    64. Paton, DJ; McGoldrick, A; Belak, S; Mittelholzer, C; Koenen, F; Vanderhallen, H; Biagetti, M; De Mia, GM; Stadejek, T; Hofmann, MA; Thuer, B
      Classical swine fever virus: a ring test to evaluate RT-PCR detection methods

      VETERINARY MICROBIOLOGY
    65. Ogiso, Y; Ueno, M; Fujimori, M; Fukushima, Y; Katsuyama, T
      A novel non-pathogenetic polymorphism of the APC gene in a patient with familial adenomatous polyposis coli

      JAPANESE JOURNAL OF CLINICAL ONCOLOGY
    66. Aihara, T; Fujiwara, Y; Miyake, Y; Okami, J; Okada, Y; Iwao, K; Sugita, Y; Tomita, N; Sakon, M; Shiozaki, H; Monden, M
      Mammaglobin B gene as a novel marker for lymph node micrometastasis in patients with abdominal cancers

      CANCER LETTERS
    67. Witters, I; Devriendt, K; Moerman, P; van Hole, C; Fryns, JP
      Diaphragmatic hernia as the first echographic sign in Apert syndrome

      PRENATAL DIAGNOSIS
    68. Glenn, CC; Deng, G; Michaelis, RC; Tarleton, J; Phelan, MC; Surh, L; Yang, TP; Driscoll, DJ
      DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprinting

      PRENATAL DIAGNOSIS
    69. Lohr, M; Maisonneuve, P; Lowenfels, AB
      K-Ras mutations and benign pancreatic disease

      INTERNATIONAL JOURNAL OF PANCREATOLOGY
    70. Bousalem, M; Dallot, S; Guyader, S
      The use of phylogenetic data to develop molecular tools for the detection and genotyping of Yam mosaic virus. Potential application in molecular epidemiology

      JOURNAL OF VIROLOGICAL METHODS
    71. Fridman, C; Koiffmann, CP
      Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    72. Yokoyama, Y; Teraoka, M; Tsuji, K; Ninomiya, S; Inoue, C; Yamashita, S; Narahara, K; Seino, Y
      Rapid screening method to detect mutations in CYP21, the gene for 21-hydroxylase

      AMERICAN JOURNAL OF MEDICAL GENETICS
    73. Fridman, C; Varela, MC; Kok, F; Diament, A; Koiffmann, CP
      Paternal UPD15: Further genetic and clinical studies in four Angelman syndrome patients

      AMERICAN JOURNAL OF MEDICAL GENETICS
    74. Ming, JE; Blagowidow, N; Knoll, JHM; Rollings, L; Fortina, P; McDonald-McGinn, DM; Spinner, NB; Zackai, EH
      Submicroscopic deletion in cousins with Prader-Willi syndrome causes a grandmatrilineal inheritance pattern: Effects of imprinting

      AMERICAN JOURNAL OF MEDICAL GENETICS
    75. Suzuki, Y; Sasagawa, I; Yazawa, H; Tateno, T; Nakada, T
      Detection of chromosome 15 deletion in Prader-Willi syndrome using fluorescence in situ hybridization

      ARCHIVES OF ANDROLOGY
    76. Tickoo, SK; Lee, MW; Eble, JN; Amin, M; Christopherson, T; Zarbo, RJ; Amin, MB
      Ultrastructural observations on mitochondria and microvesicles in renal oncocytoma, chromophobe renal cell carcinoma, and eosinophilic variant of conventional (clear cell) renal cell carcinoma

      AMERICAN JOURNAL OF SURGICAL PATHOLOGY
    77. Lin, YM; Chen, CW; Sun, HS; Hsu, CC; Chen, JM; Lin, SJ; Lin, JSN; Kuo, PL
      Y-chromosome microdeletion and its effect on reproductive decisions in Taiwanese patients presenting with nonobstructive azoospermia

      UROLOGY
    78. Ladanyi, M; Bridge, JA
      Contribution of molecular genetic data to the classification of sarcomas

      HUMAN PATHOLOGY
    79. Pivnik, AV; Pustovoit, YS; Karpova, IV; Surin, VL; Lukyanenko, AV
      Pilot results of detection of mutations in the gene of the enzyme porphobilinogen-desaminase inpatients with acute intermittent porphyria in Russia

      TERAPEVTICHESKII ARKHIV
    80. de la Herran, R; Garrido-Ramos, MA; Navas, JI; Rejon, CR; Rejon, MR
      Molecular characterization of the ribosomal RNA gene region of Perkinsus atlanticus: its use in phylogenetic analysis and as a target for a moleculardiagnosis

      PARASITOLOGY
    81. Felice, KJ; North, WA; Moore, SA; Mathews, KD
      FSH dystrophy 4q35 deletion in patients presenting with facial-sparing scapular myopathy

      NEUROLOGY
    82. van der Kooi, AJ; Visser, MC; Rosenberg, N; van den Berg-Vos, R; Wokke, JHJ; Bakker, E; de Visser, M
      Extension of the clinical range of facioscapulohumeral dystrophy: report of six cases

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    83. Kerstens, HMJ; Robben, JCM; Poddighe, PJ; Melchers, WJG; Boonstra, H; de Wilde, PCM; Macville, MVE; Hanselaar, AGJM
      AgarCyto: A novel cell-processing method for multiple molecular diagnosticanalyses of the uterine cervix

      JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY
    84. Caccio, C; Camma, C; Onuma, M; Severini, C
      The beta-tubulin gene of Babesia and Theileria parasites is an informativemarker for species discrimination

      INTERNATIONAL JOURNAL FOR PARASITOLOGY
    85. McEntagart, ME; Webb, T; Hardy, C; King, MD
      Familial Prader-Willi syndrome: Case report and a literature review

      CLINICAL GENETICS
    86. Westbrook, CA; Hsu, WT; Chyna, B; Litvak, D; Raza, A; Horrigan, SK
      Cytogenetic and molecular diagnosis of chromosome 5 deletions in myelodysplasia

      BRITISH JOURNAL OF HAEMATOLOGY
    87. Cerveira, N; Ferreira, S; Doria, S; Veiga, I; Ferreira, F; Martz, JM; Marques, M; Castedo, S
      Detection of prognostic significant translocations in childhood acute lymphoblastic leukaemia by one-step multiplex reverse transcription polymerase chain reaction

      BRITISH JOURNAL OF HAEMATOLOGY
    88. Takano, T; Hasegawa, Y; Matsuzuka, F; Miyauchi, A; Yoshida, H; Higashiyama, T; Kuma, K; Amino, N
      Gene expression profiles in thyroid carcinomas

      BRITISH JOURNAL OF CANCER
    89. Sprouse, JT; Werling, R; Hanke, D; Lakey, C; McDonnel, L; Wood, BL; Sabath, DE
      T-cell clonality determination using polymerase chain reaction (PCR) amplification of the T-cell receptor gamma-chain gene and capillary electrophoresis of fluorescently labeled PCR products

      AJCP. American journal of clinical pathology
    90. Bartlett, JMS; Adie, L; Watters, AD; Going, JJ; Grigor, KM
      Chromosomal aberrations in transitional cell carcinoma that are predictiveof disease outcome are independent of polyploidy

      BJU INTERNATIONAL
    91. Tanaka, A; Fujimaru, M; Choeh, K; Isshiki, G
      Novel mutations including the second most common in Japan, in the beta-hexosaminidase alpha subunit gene, and a simple screening of Japanese patientswith Tay-Sachs disease

      JOURNAL OF HUMAN GENETICS
    92. Shimizu, N; Nakazono, H; Takeshita, Y; Ikeda, C; Fujii, H; Watanabe, A; Yamaguchi, Y; Hemmi, H; Shimatake, H; Aoki, T
      Molecular analysis and diagnosis in Japanese patients with Wilson's disease

      PEDIATRICS INTERNATIONAL
    93. Yasui, W; Yokozaki, H; Shimamoto, F; Tahara, H; Tahara, E
      Molecular-pathological diagnosis of gastrointestinal tissues and its contribution to cancer histopathology

      PATHOLOGY INTERNATIONAL
    94. Muralidhar, B; Marney, A; Butler, MG
      Analysis of imprinted genes in subjects with Prader-Willi syndrome and chromosome 15 abnormalities

      GENETICS IN MEDICINE
    95. Ramachandran, C; Melnick, SJ
      Multidrug resistance review in human tumors - Molecular diagnosis and clinical significance

      MOLECULAR DIAGNOSIS
    96. Krafft, AE; Taubenberger, JK; Sheng, ZM; Bijwaard, KE; Abbondanzo, SL; Aguilera, NSI; Lichy, JH
      Enhanced sensitivity with a novel TCR gamma PCR assay for clonality studies in 569 formalin-fixed, paraffin-embedded (FFPE) cases

      MOLECULAR DIAGNOSIS
    97. Carrel, AL; Huber, S; Allen, DB; Voelkerding, KV
      Assessment of SNRPN expression as a molecular tool in the diagnosis of Prader-Willi syndrome

      MOLECULAR DIAGNOSIS
    98. da Silva, AJ; Bornay-Llinares, FJ; Moura, INS; Slemenda, SB; Tuttle, JL; Pieniazek, NJ
      Fast and reliable extraction of protozoan parasite DNA from fecal specimens

      MOLECULAR DIAGNOSIS
    99. El-Naggar, AK
      Diagnostic molecular pathology comes of age

      ADVANCES IN ANATOMIC PATHOLOGY
    100. Feriotto, G; Lucci, M; Bianchi, N; Mischiati, C; Gambari, R
      Detection of the Delta F508 (F508del) mutation of the cystic fibrosis geneby surface plasmon resonance and biosensor technology

      HUMAN MUTATION


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Documento generato il 20/10/20 alle ore 02:35:40